Carbone A, Cilia A M, Gloghini A, Capello D, Todesco M, Quattrone S, Volpe R, Gaidano G
Division of Pathology, Centro di Riferimento Oncologico, IRCCS, Istituto Nazionale Tumori, Aviano, Italy.
Br J Haematol. 1998 Sep;102(4):1081-9. doi: 10.1046/j.1365-2141.1998.00877.x.
In this study we report on the establishment and characterization of two novel lymphoma cell lines (CRO-AP/3 and CRO-AP/5) which carry infection by human herpesvirus type-8 (HHV-8) and have derived from AIDS-related primary effusion lymphoma (PEL). These two cell lines are representative of different virologic subtypes of PEL, i.e. HHV-8+/EBV- PEL in the case of CRO-AP/3 and HHV-8+/EBV+ PEL in the case of CRO-AP/5. Consistent with the diagnosis of PEL, both CRO-AP/3 and CRO-AP/5 expressed indeterminate (i.e. non-B, non-T) phenotypes although immunogenotypic studies documented their B-cell origin. Both cell lines are devoid of genetic lesions of c-MYC, BCL-2 and p53 as well as gross rearrangements of BCL-6. Detailed histogenetic characterization of these novel PEL cell lines suggests that PEL may derive from a post-germinal centre B cell which has undergone pre-terminal differentiation. The CRO-AP/3 and CRO-AP/5 cell lines may provide a valuable model for clarifying the pathogenesis of PEL. In particular, these cell lines may help understand the relative contribution of HHV-8 and EBV to PEL growth and development and may facilitate the identification of recurrent cytogenetic abnormalities highlighting putative novel cancer related loci relevant to PEL.
在本研究中,我们报告了两种新型淋巴瘤细胞系(CRO-AP/3和CRO-AP/5)的建立及其特征,这两种细胞系感染了人类8型疱疹病毒(HHV-8),源自艾滋病相关原发性渗出性淋巴瘤(PEL)。这两种细胞系代表了PEL的不同病毒学亚型,即CRO-AP/3为HHV-8+/EBV- PEL,CRO-AP/5为HHV-8+/EBV+ PEL。与PEL的诊断一致,CRO-AP/3和CRO-AP/5均表现出不确定(即非B、非T)表型,尽管免疫基因分型研究证明它们起源于B细胞。两种细胞系均无c-MYC、BCL-2和p53的基因损伤以及BCL-6的大规模重排。对这些新型PEL细胞系的详细组织发生学特征分析表明,PEL可能源自已发生终末前分化的生发中心后B细胞。CRO-AP/3和CRO-AP/5细胞系可能为阐明PEL的发病机制提供有价值的模型。特别是,这些细胞系可能有助于了解HHV-8和EBV对PEL生长和发展的相对贡献,并可能有助于识别复发性细胞遗传学异常,突出与PEL相关的假定新型癌症相关基因座。